Understanding How Turfgrass Herbicides Work

Total Page:16

File Type:pdf, Size:1020Kb

Understanding How Turfgrass Herbicides Work W 352 Understanding How Turfgrass Herbicides Work Gregory K. Breeden, UT Extension Specialist, Turfgrass Weed Science James T. Brosnan, Associate Professor, Turfgrass Weed Science Javier Vargas, Research Associate, Turfgrass Weed Science Department of Plant Sciences Herbicides are chemicals that inhibit normal other agricultural systems. Developing weed plant growth processes resulting in death of management programs utilizing herbicides that susceptible weeds. The processes by which employ different mechanisms of action is critical to herbicides kill weeds are called modes of action while both preventing and managing herbicide resistant the location where these effects occur at the cellular weeds. It is recommended to rotate herbicides that level is termed the site of action or the mechanism of employ different mechanisms of action as often as action. The Weed Science Society of America (WSSA) possible, as well as implementing cultural practices uses a numerical system to group herbicides by that maximize turf competition and limit weed mechanism of action. A more detailed description of encroachment. Table 2 lists single active ingredient this numerical system is presented in Table 1. herbicides used in turfgrass by mechanisms of action Continual reliance on herbicides that employ the group number. These WSSA group numbers can also same mechanism of action has led to the evolution of be found on most herbicide labels as well (Figure 1). herbicide-resistant weeds in turfgrass, as well as in Figure 1. The Weed Society of America (WSSA) uses a numerical system to group herbicides by mechanism of action. The WSSA group number can be found on most herbicide labels. Table 1. Mechanisms for action of herbicides used to control weeds in turfgrass. WSSA Action Mechanism of Action Description Group 1 Acetyl CoA Carboxylase Inhibit synthesis of fatty acids required for building new cell (ACCase) Inhibitor membranes 2 Acetolactate Synthase Inhibit the acetolactate synthase (ALS) enzyme involved in (ALS) Inhibitor synthesizing branch chain amino acids such as isoleucine, leucine and valine 3 Microtubule Inhibitor Inhibit microtubule structure and function during cell division 4 Synthetic Auxin Act similar to endogenous auxin (IAA) causing uncontrolled cell division and growth that damages vascular tissue 5, 6 & 7 Photosystem II Inhibitor Inhibit proper electron flow during the light reactions of photosynthesis (i.e., photosystem II) 8 & 16 Lipid Biosynthesis Inhibit synthesis of fatty acids and lipids Inhibitor 9 EPSP Synthase Inhibitor Inhibit production of aromatic amino acids (tryptophan, tyrosine and phenylalanine) required for protein synthesis 10 Glutamine Synthetase Inhibits conversion of glutamate and ammonia to glutamine Inhibitor 14 Protoporphyrinogen Inhibit the PPO enzyme involved in chlorophyll and heme Oxidase (PPO) Inhibitor synthesis 15 Long Chain Fatty Acid Inhibit very long chain fatty acid synthesis Inhibitor 17 Specific Site Unknown The mechanism of action for these herbicides remains unknown, but could potentially be nucleic acid inhibitors 21 & 29 Cellulose biosynthesis Inhibit cell wall synthesis inhibitor (CBI) 22 Photosystem I Inhibitor Herbicides accept electrons from photsystem I leading to oxidative stress that damages cellular structures 26 Specific Site Unknown The mechanism of action for these herbicides remains unknown 27 Carotenoid Biosynthesis Inhibit synthesis of carotenoid pigments that protect chlorophyll Inhibitor from oxidative stress Table 2. Single herbicide active ingredients labeled for use in turfgrass. WSSA Action Ex. Trade Mode of Action Mechanism of Action Group Chemical Family Active Ingredient Names Lipid Biosynthesis Acetyl CoA Carboxylase 1 Aryloxyphenoxy-propionate fenoxaprop Acclaim Extra Inhibitor (ACCase) Inhibitor (FOPs) fluazifop Fusilade II Cyclohexanedione (DIMs) sethoxydim Segment Amino Acid Synthesis Acetolactate Synthase 2 Sulfonylurea chlorsulfuron Corsair Inhibitor (ALS) Inhibitor flazasulfuron Katana foramsulfuron Revolver halosulfuron SedgeHammer imazosulfuron Celero iodosulfuron *NA metsulfuron Manor rimsulfuron TranXit sulfosulfuron Certainty trifloxysulfuron Monument Sulfonylaminocarbonyltriazolinone thiencarbazone *NA Imidazolinone imazaquin Image imazapic Plateau Triazolopyrimidine florasulam Defendor penoxsulam Lockup Pyrimidinyl(thio)benzoate bispyribac-sodium Velocity Root Growth Inhibitor Microtubule Inhibitor 3 Dinitroaniline benefin Balan oryzalin Surflan pendimethalin Pendulum prodiamine Barricade trifluralin Treflan Pyridine dithiopyr Dimension Benzamide pronamide Kerb Phthalic Acid DCPA *NA WSSA Action Ex. Trade Mode of Action Mechanism of Action Group Chemical Family Active Ingredient Names Synthetic Auxin Not Well Understood 4 Phenoxy 2,4-D Various MCPP MCPA 2,4-DB Benzoic Acid dicamba Banvel Pyridine Carboxylic Acid clopyralid Lontrel fluroxypyr *NA triclopyr Garlon 4 & 26** Quinoline Carboxylic Acid quinclorac Drive XLR8 Photosynthesis Photosystem II Inhibitor 5 Triazine atrazine AAtrex Inhibitor simazine Princep Triazinone metribuzin Sencor Triazolinone amicarbizone Xonerate Photosynthesis Photosystem II Inhibitor 6 Nitrile bromoxynil Buctril Inhibitor Benzothiadiazinone bentazon Basagran Photosynthesis Photosystem II Inhibitor 7 Urea siduron Tupersan Inhibitor Lipid Biosynthesis Not Well Understood 8 Phosphorodithioate bensulide Bensumec Inhibitor Amino Acid Synthesis EPSP Synthase Inhibitor 9 Glycine glyphosate Roundup Pro Inhibitor Nitrogen Metabolism Glutamine Synthetase 10 Phosphinic Acid glufosinate-ammonium Finale Inhibitor Cell Membrane Protoporphyrinogen Oxidase 14 Aryl Triazinone carfentrazone Quicksilver Disrupter (PPO) Inhibitor sulfentrazone Dismiss N-phenylphthalimide flumioxazin Sureguard Oxadiazole oxadiazon Ronstar Pyrazole pyraflufen-ethyl Octane Shoot Growth Inhibitor Long Chain Fatty Acid 15 Chloroacetamide dimethenamid Tower Inhibitor metolachlor Pennant WSSA Action Ex. Trade Mode of Action Mechanism of Action Group Chemical Family Active Ingredient Names Lipid Biosynthesis Not Well Understood 16 Benzofuran ethofumesate Prograss Inhibitor Not Well Understood Not Well Understood 17 Organic Arsenical monosodium Various methanearsonate (MSMA) Dihydropter-oate Not Well Understood 18 Carbamate asulam Asulox (DHP) Synthase Inhibitor Cellulose Biosynthesis Cell Wall Biosynthesis 21 Benzamide isoxaben Gallery Inhibitor (CBI) Inhibitor Cell Membrane Photosystem I Inhibitor 22 Bipyridilium diquat Reward Disrupter Not Well Understood Not Well Understood 26 & 4** Quinoline Carboxylic Acid quinclorac Drive XLR8 26 Dithiocarbamate dazomet Basamid Carotenoid 4-Hydroxyphenyl-Pyruvate- 27 Triketone mesotrione Tenacity Biosynthesis Inhibitor Dioxygenase (HPPD) Inhibitor Pyrazolone topramezone Pylex Cellulose Biosynthesis Cellulose Biosynthesis 29 Alkylazine indaziflam Specticle Inhibitor (CBI) Inhibitor *NA = Not available alone, but can be found in numerous mixtures. **Quinclorac WSSA action groups are 4 for dicots and 26 for monocots. In turfgrass, multiple active ingredients are often recommended when these materials are applied sold commercially as pre-packaged mixtures to alone (i.e., not in a mixture). Table 3 lists example broaden the spectrum of weeds controlled by a single herbicides labeled for use in turfgrass that contain herbicide application. While these products are very multiple active ingredients and the corresponding useful tools for weed control, they do not replace the WSSA group number for each. Figure 2 is an example need to rotate to herbicides with other mechanisms of how these groups may be represented on the of action because active ingredients in these mixtures product label. are often included at rates lower than what would be Figure 2. Some herbicides labeled for use in turfgrass contain multiple active ingredients from various WSSA groups, as shown on the above label. Table 3. Select herbicides labeled for use in turfgrass that contain multiple active ingredients. Trade Name(s) Active Ingredients WSSA Action Groups 2DQ 2,4-D + dicamba + quinclorac 4 + 4 + (26 or 4) 4-Speed XT 2,4-D + triclopyr + dicamba + pyraflufen-ethyl 4 + 4 + 4 + 14 Anderson’s Goosegrass/Crabgrass oxadiazon + dithiopyr 14 + 3 Blindside sulfentrazone + metsulfuron 14 + 2 Brushmaster 2,4-D + 2,4-DB + dicamba 4 + 4 + 4 Celsius thiencarbazone + iodosulfuron + dicamba 2 + 2 + 4 ChangeUp MCPA + fluroxypyr + dicamba 4 + 4 + 4 Confront, 2D triclopyr + clopyralid 4 + 4 Coolpower, Horsepower, Eliminate MCPA + triclopyr + dicamba 4 + 4 + 4 Dismiss South sulfentrazone + imazethapyr 14 + 2 Echelon sulfentrazone + prodiamine 14 + 3 Escalade 2 2,4-D + fluroxypyr + dicamba 4 + 4 + 4 Freehand dimethenamid + pendimethalin 15 + 3 Last Call fenoxaprop + fluroxypyr + dicamba 1 + 4 + 4 Millennium Ultra 2 2,4-D + clopyralid + dicamba 4 + 4 + 4 Momentum FX2 2,4-D + triclopyr + fluroxypyr 4 + 4 + 4 Negate metsulfuron + rimsulfuron 2 + 2 Powerzone carfentrazone + MCPA + MCPP + dicamba 14 + 4 + 4 + 4 ProDeuce glyphosate + prodiamine 9 + 3 Trade Name(s) Active Ingredients WSSA Action Groups Q-4 Plus quinclorac + sulfentrazone + 2,4-D + dicamba (26 or 4) + 14 + 4 + 4 QuickPro glyphosate + diquat 9 + 22 Solitare sulfentrazone + quinclorac 14 + (26 or 4) Specticle Total indaziflam + glyphosate + diquat 29 + 9 + 22 Speedzone carfentrazone + 2,4-D + MCPP + dicamba 14 + 4 + 4 + 4 Squareone carfentrazone + quinclorac 14 + (26 or 4) Surge, Surezone sulfentrazone + 2,4-D + MCPP + dicamba 14 + 4 + 4 + 4 Tribute Total thiencarbazone + foramsulfuron + halosulfuron 2 + 2 + 2 Trimec
Recommended publications
  • Restricted Use Product Summary Report
    Page 1 of 17 Restricted Use Product Summary Report (January 19, 2016) Percent Active Registration # Name Company # Company Name Active Ingredient(s) Ingredient 4‐152 BONIDE ORCHARD MOUSE BAIT 4 BONIDE PRODUCTS, INC. 2 Zinc phosphide (Zn3P2) 70‐223 RIGO EXOTHERM TERMIL 70 VALUE GARDENS SUPPLY, LLC 20 Chlorothalonil 100‐497 AATREX 4L HERBICIDE 100 SYNGENTA CROP PROTECTION, LLC 42.6 Atrazine 100‐585 AATREX NINE‐O HERBICIDE 100 SYNGENTA CROP PROTECTION, LLC 88.2 Atrazine 100‐669 CURACRON 8E INSECTICIDE‐MITICIDE 100 SYNGENTA CROP PROTECTION, LLC 73 Profenofos 100‐817 BICEP II MAGNUM HERBICIDE 100 SYNGENTA CROP PROTECTION, LLC 33; 26.1 Atrazine; S‐Metolachlor 100‐827 BICEP LITE II MAGNUM HERBICIDE 100 SYNGENTA CROP PROTECTION, LLC 28.1; 35.8 Atrazine; S‐Metolachlor 100‐886 BICEP MAGNUM 100 SYNGENTA CROP PROTECTION, LLC 33.7; 26.1 Atrazine; S‐Metolachlor 100‐898 AGRI‐MEK 0.15 EC MITICIDE/INSECTICIDE 100 SYNGENTA CROP PROTECTION, LLC 2 Abamectin 100‐903 DENIM INSECTICIDE 100 SYNGENTA CROP PROTECTION, LLC 2.15 Emamectin benzoate 100‐904 PROCLAIM INSECTICIDE 100 SYNGENTA CROP PROTECTION, LLC 5 Emamectin benzoate 100‐998 KARATE 1EC 100 SYNGENTA CROP PROTECTION, LLC 13.1 lambda‐Cyhalothrin 100‐1075 FORCE 3G INSECTICIDE 100 SYNGENTA CROP PROTECTION, LLC 3 Tefluthrin Acetochlor; Carbamothioic acid, dipropyl‐ 100‐1083 DOUBLEPLAY SELECTIVE HERBICIDE 100 SYNGENTA CROP PROTECTION, LLC 16.9; 67.8 , S‐ethyl ester 100‐1086 KARATE EC‐W INSECTICIDE 100 SYNGENTA CROP PROTECTION, LLC 13.1 lambda‐Cyhalothrin 100‐1088 SCIMITAR GC INSECTICIDE 100 SYNGENTA CROP PROTECTION,
    [Show full text]
  • (12) United States Patent (10) Patent No.: US 8,586,504 B2 Wright Et Al
    USOO85865.04B2 (12) United States Patent (10) Patent No.: US 8,586,504 B2 Wright et al. (45) Date of Patent: Nov. 19, 2013 (54) HERBICIDAL COMPOSITIONS CONTAINING FOREIGN PATENT DOCUMENTS GLYPHOSATE AND A PYRONE ANALOG AU 100.73/92 B 10, 1992 CA 2340240 A1 2, 2000 (75) Inventors: Daniel R. Wright, St. Louis, MO (US); EP O 808 569 A1 11, 1997 Joseph J. Sandbrink, Chesterfield, MO GB 2267 825 A 12/1993 (US); Paul G. Ratliff, Olivette, MO WO 99/00013 1, 1999 WO OO,30452 6, 2000 (US) WO OO,642.57 11, 2000 WO OO/67571 11, 2000 (73) Assignee: Monsanto Technology LLC, St. Louis, WO O1/35740 A2 5, 2001 MO (US) WO 02/21924 A2 3, 2002 (*) Notice: Subject to any disclaimer, the term of this OTHER PUBLICATIONS patent is extended or adjusted under 35 Exhibit PMH-17 Supplemental Labeling regarding Roundup Pro U.S.C. 154(b) by 0 days. Herbicide by Monsanto, EPA Reg. No. 524-475 (Nov. 1995), 11 pageS. (21) Appl. No.: 13/404,861 Exhibit PMH-18 Notice of Pesticide Registration issued on Oct. 5, 2000, 35 pages. Exhibit PMH-19 EPA Application for Pesticide, ID No. 200405 (22) Filed: Feb. 24, 2012 (Sep. 1995), 33 pages. Exhibit PMH-20-Documentation regarding Starmas Racun/ (65) Prior Publication Data Rumpai Herbicide (bears the year 2003), 10 pages. Exhibit PMH-21—Documentation regarding Starmix Racun/ US 2012/O157309 A1 Jun. 21, 2012 Rumpai Herbicide (Date Unknown), 3 pages. Exhibit PMH-22—article entitled Control of Eucalyptus grandis cut stumps by Keith Little et al., ICFR Bulletin Series, No.
    [Show full text]
  • 2,4-Dichlorophenoxyacetic Acid
    2,4-Dichlorophenoxyacetic acid 2,4-Dichlorophenoxyacetic acid IUPAC (2,4-dichlorophenoxy)acetic acid name 2,4-D Other hedonal names trinoxol Identifiers CAS [94-75-7] number SMILES OC(COC1=CC=C(Cl)C=C1Cl)=O ChemSpider 1441 ID Properties Molecular C H Cl O formula 8 6 2 3 Molar mass 221.04 g mol−1 Appearance white to yellow powder Melting point 140.5 °C (413.5 K) Boiling 160 °C (0.4 mm Hg) point Solubility in 900 mg/L (25 °C) water Related compounds Related 2,4,5-T, Dichlorprop compounds Except where noted otherwise, data are given for materials in their standard state (at 25 °C, 100 kPa) 2,4-Dichlorophenoxyacetic acid (2,4-D) is a common systemic herbicide used in the control of broadleaf weeds. It is the most widely used herbicide in the world, and the third most commonly used in North America.[1] 2,4-D is also an important synthetic auxin, often used in laboratories for plant research and as a supplement in plant cell culture media such as MS medium. History 2,4-D was developed during World War II by a British team at Rothamsted Experimental Station, under the leadership of Judah Hirsch Quastel, aiming to increase crop yields for a nation at war.[citation needed] When it was commercially released in 1946, it became the first successful selective herbicide and allowed for greatly enhanced weed control in wheat, maize (corn), rice, and similar cereal grass crop, because it only kills dicots, leaving behind monocots. Mechanism of herbicide action 2,4-D is a synthetic auxin, which is a class of plant growth regulators.
    [Show full text]
  • USDA, Forest Service Forest Health Protection GSA Contract No
    SERA TR 02-43-13-03b Triclopyr - Revised Human Health and Ecological Risk Assessments Final Report Prepared for: USDA, Forest Service Forest Health Protection GSA Contract No. GS-10F-0082F USDA Forest Service BPA: WO-01-3187-0150 USDA Purchase Order No.: 43-1387-2-0245 Task No. 13 Submitted to: Dave Thomas, COTR Forest Health Protection Staff USDA Forest Service Rosslyn Plaza Building C, Room 7129C 1601 North Kent Street Arlington, VA 22209 Submitted by: Patrick R. Durkin Syracuse Environmental Research Associates, Inc. 5100 Highbridge St., 42C Fayetteville, New York 13066-0950 Telephone: (315) 637-9560 Fax: (315) 637-0445 E-Mail: [email protected] Home Page: www.sera-inc.com March 15, 2003 TABLE OF CONTENTS LIST OF APPENDICES ...................................................... iv LIST OF WORKSHEETS ...................................................... v LIST OF ATTACHMENTS .................................................... v LIST OF TABLES ............................................................ v LIST OF FIGURES ......................................................... viii ACRONYMS, ABBREVIATIONS, AND SYMBOLS .............................. ix COMMON UNIT CONVERSIONS AND ABBREVIATIONS ......................... xi CONVERSION OF SCIENTIFIC NOTATION .................................... xii EXECUTIVE SUMMARY ................................................... xiii 1. INTRODUCTION ........................................................ 1-1 2. PROGRAM DESCRIPTION ................................................ 2-1 2.1. OVERVIEW
    [Show full text]
  • Herbicide Mode of Action Table High Resistance Risk
    Herbicide Mode of Action Table High resistance risk Chemical family Active constituent (first registered trade name) GROUP 1 Inhibition of acetyl co-enzyme A carboxylase (ACC’ase inhibitors) clodinafop (Topik®), cyhalofop (Agixa®*, Barnstorm®), diclofop (Cheetah® Gold* Decision®*, Hoegrass®), Aryloxyphenoxy- fenoxaprop (Cheetah®, Gold*, Wildcat®), fluazifop propionates (FOPs) (Fusilade®), haloxyfop (Verdict®), propaquizafop (Shogun®), quizalofop (Targa®) Cyclohexanediones (DIMs) butroxydim (Factor®*), clethodim (Select®), profoxydim (Aura®), sethoxydim (Cheetah® Gold*, Decision®*), tralkoxydim (Achieve®) Phenylpyrazoles (DENs) pinoxaden (Axial®) GROUP 2 Inhibition of acetolactate synthase (ALS inhibitors), acetohydroxyacid synthase (AHAS) Imidazolinones (IMIs) imazamox (Intervix®*, Raptor®), imazapic (Bobcat I-Maxx®*, Flame®, Midas®*, OnDuty®*), imazapyr (Arsenal Xpress®*, Intervix®*, Lightning®*, Midas®* OnDuty®*), imazethapyr (Lightning®*, Spinnaker®) Pyrimidinyl–thio- bispyribac (Nominee®), pyrithiobac (Staple®) benzoates Sulfonylureas (SUs) azimsulfuron (Gulliver®), bensulfuron (Londax®), chlorsulfuron (Glean®), ethoxysulfuron (Hero®), foramsulfuron (Tribute®), halosulfuron (Sempra®), iodosulfuron (Hussar®), mesosulfuron (Atlantis®), metsulfuron (Ally®, Harmony®* M, Stinger®*, Trounce®*, Ultimate Brushweed®* Herbicide), prosulfuron (Casper®*), rimsulfuron (Titus®), sulfometuron (Oust®, Eucmix Pre Plant®*, Trimac Plus®*), sulfosulfuron (Monza®), thifensulfuron (Harmony®* M), triasulfuron (Logran®, Logran® B-Power®*), tribenuron (Express®),
    [Show full text]
  • Exposure to Herbicides in House Dust and Risk of Childhood Acute Lymphoblastic Leukemia
    Journal of Exposure Science and Environmental Epidemiology (2013) 23, 363–370 & 2013 Nature America, Inc. All rights reserved 1559-0631/13 www.nature.com/jes ORIGINAL ARTICLE Exposure to herbicides in house dust and risk of childhood acute lymphoblastic leukemia Catherine Metayer1, Joanne S. Colt2, Patricia A. Buffler1, Helen D. Reed3, Steve Selvin1, Vonda Crouse4 and Mary H. Ward2 We examine the association between exposure to herbicides and childhood acute lymphoblastic leukemia (ALL). Dust samples were collected from homes of 269 ALL cases and 333 healthy controls (o8 years of age at diagnosis/reference date and residing in same home since diagnosis/reference date) in California, using a high-volume surface sampler or household vacuum bags. Amounts of agricultural or professional herbicides (alachlor, metolachlor, bromoxynil, bromoxynil octanoate, pebulate, butylate, prometryn, simazine, ethalfluralin, and pendimethalin) and residential herbicides (cyanazine, trifluralin, 2-methyl-4- chlorophenoxyacetic acid (MCPA), mecoprop, 2,4-dichlorophenoxyacetic acid (2,4-D), chlorthal, and dicamba) were measured. Odds ratios (OR) and 95% confidence intervals (CI) were estimated by logistic regression. Models included the herbicide of interest, age, sex, race/ethnicity, household income, year and season of dust sampling, neighborhood type, and residence type. The risk of childhood ALL was associated with dust levels of chlorthal; compared to homes with no detections, ORs for the first, second, and third tertiles were 1.49 (95% CI: 0.82–2.72), 1.49 (95% CI: 0.83–2.67), and 1.57 (95% CI: 0.90–2.73), respectively (P-value for linear trend ¼ 0.05). The magnitude of this association appeared to be higher in the presence of alachlor.
    [Show full text]
  • Efficacy of Imazapic/Imazapyr and Other Herbicides in Mixtures for The
    Efficacy of imazapic/imazapyr and other herbicides in mixtures for the control of Digitaria insularis prior to soybean sowing Efectividad de imazapic/imazapyr y otros herbicidas en mezclas para el control de Digitaria insularis en pre-siembra de soya Alfredo Junior Paiola Albrecht1, Leandro Paiola Albrecht1, André Felipe Moreira Silva²*, Romulo Augusto Ramos³, Everson Pedro Zeny³, Juliano Bortoluzzi Lorenzetti4, Maikon Tiago Yamada Danilussi4, and Arthur Arrobas Martins Barroso4 ABSTRACT RESUMEN Herbicide mixtures, use of multiple sites of action, and other Las mezclas entre herbicidas, el uso de múltiples sitios de acción weed management practices are necessary to avoid cases of y otras prácticas de manejo de malezas son necesarias para biotype resistance. The aim of this study was to evaluate the evitar otros casos de resistencia de biotipos. El objetivo de este efficiency of imazapic/imazapyr and other herbicides in mix- estudio fue evaluar la eficiencia de imazapic/imazapyr y otros tures to control Digitaria insularis at burndown before soybean herbicidas en mezclas para controlar Digitaria insularis en la sowing. This field research was conducted in Umuarama, State desecación antes de la siembra de soya. Esta investigación de of Parana (PR), Brazil, in the 2018/19 soybean season. The ex- campo se realizó en Umuarama, Estado de Paraná (PR), Brasil, periment was conducted in a randomized block experimental en la cosecha de soya de 2018/19. El experimento se realizó en design with four replicates and 11 treatments composed of the un diseño experimental de bloques al azar, con cuatro repe- application of glyphosate, clethodim, haloxyfop, imazapic/ ticiones y 11 tratamientos, compuestos por la aplicación de imazapyr, glufosinate, 2,4-dichlorophenoxyacetic acid (2,4-D), glifosato, cletodim, haloxifop, imazapic/imazapir, glufosinato, dicamba, triclopyr, and saflufenacil, in mixtures.
    [Show full text]
  • Safety and Efficacy of Postemergence Herbicides for Container-Grown Landscape Groundcovers
    1 17B-Student-Conner-IPPS-2018.doc Safety and Efficacy of Postemergence Herbicides for Container-Grown Landscape Groundcovers© Crystal J. Connera, Chris Marble, and Annette Chandler Mid-Florida Research and Education Center, University of Florida, 2725 S. Binion Road, Apopka, Florida 32703, USA aEmail: [email protected] KeyWords: Landscape nursery, weed management, asiatic jasmine, Trachelospermum asiaticum ‘Minima’, perennial peanut, Arachis glabrata ‘Ecoturf’ SUMMARY Research was conducted to determine crop tolerance of asiatic jasmine (Trachelospermum asiaticum ‘Minima’) and perennial peanut (Arachis glabrata ‘Ecoturf’) to postemergence herbicides including bentazon, sulfentrazone, iron HEDTA, indaziflam (a preemergence herbicide), sulfosulfuron, and clopyralid. Efficacy of these herbicides was evaluated on flowering eclipta (Eclipta prostrata) and hairy beggarticks (Bidens pilosa). All herbicides with the exception of bentazon caused no significant damage to asiatic jasmine; injury resulting from bentazon was minimal. In perennial peanut, the highest injury was noted in plants treated with indaziflam, sulfosulfuron, or clopyralid, but injury was less than 30% and considered acceptable. All herbicides evaluated provided poor control of either weed species with the exception of clopyralid, which provided over 90% control of hairy beggarticks. Results indicate that several postemergence herbicides labeled for use in either nurseries or landscapes could be used to manage weeds in asiatic jasmine or perennial peanut groundcovers but further testing is needed. 1 2 INTRODUCTION Turfgrass is the most widely planted irrigated crop in the United States and occupies the vast majority of most residential and commercial landscapes in Florida (NTRI, 2003). However, the common mantra of landscape design is “right plant right place”. In many neighborhoods, parks, and other areas containing significant tree canopy, turfgrass is not suitable due to limited sunlight.
    [Show full text]
  • Weed Management with Diclosulam in Peanut (Arachis Hypogaea)1
    Weed Technology. 2002. Volume 16:724–730 Weed Management with Diclosulam in Peanut (Arachis hypogaea)1 ANDREW J. PRICE, JOHN W. WILCUT, and CHARLES W. SWANN2 Abstract: Field experiments were conducted at three locations in North Carolina in 1998 and 1999 and one location in Virginia in 1998 to evaluate weed management systems in peanut. Treatments consisted of diclosulam alone preemergence (PRE), or diclosulam plus metolachlor PRE alone or followed by (fb) bentazon plus acifluorfen postemergence (POST). These systems were also com­ pared with commercial standards of metolachlor PRE fb bentazon plus acifluorfen POST or imazapic POST. Our data indicate that diclosulam PRE plus metolachlor PRE in conventional tillage peanut production usually controlled common lambsquarters, common ragweed, prickly sida, and entireleaf morningglory. But control of spurred anoda, goosegrass, ivyleaf morningglory, large crabgrass, and pitted morningglory by this system was inconsistent and may require additional POST herbicide treatments. Systems that included diclosulam plus metolachlor PRE consistently provided high yields and net returns. Nomenclature: Acifluorfen, bentazon, diclosulam, imazapic, metolachlor; common lambsquarters, Chenopodium album L. #3 CHEAL; common ragweed, Ambrosia artemisiifolia L. # AMBEL; enti­ releaf morningglory, Ipomoea hederacea var. integruiscula Grey # IPOHG; goosegrass, Eleusine indica (L.) Gaertn. # ELEIN; ivyleaf morningglory, Ipomoea hederacea (L.) Jacq # IPOHE; large crabgrass, Digitaria sanguinalis L. Scop. # DIGSA; pitted morningglory, Ipomoea lacunosa L. # IPOLA; prickly sida, Sida spinosa L. # SIDSP; spurred anoda, Anoda cristata L. # ANVCR; peanut, Arachis hypogaea L. ‘NC 10C’, ‘NC 12C’. Additional index words: Economic analysis. Abbreviations: fb, followed by; POST, postemergence; PPI, preplant incorporated; PRE, preemer­ gence. INTRODUCTION Wilcut and Swann 1990; Wilcut et al.
    [Show full text]
  • INDEX to PESTICIDE TYPES and FAMILIES and PART 180 TOLERANCE INFORMATION of PESTICIDE CHEMICALS in FOOD and FEED COMMODITIES
    US Environmental Protection Agency Office of Pesticide Programs INDEX to PESTICIDE TYPES and FAMILIES and PART 180 TOLERANCE INFORMATION of PESTICIDE CHEMICALS in FOOD and FEED COMMODITIES Note: Pesticide tolerance information is updated in the Code of Federal Regulations on a weekly basis. EPA plans to update these indexes biannually. These indexes are current as of the date indicated in the pdf file. For the latest information on pesticide tolerances, please check the electronic Code of Federal Regulations (eCFR) at http://www.access.gpo.gov/nara/cfr/waisidx_07/40cfrv23_07.html 1 40 CFR Type Family Common name CAS Number PC code 180.163 Acaricide bridged diphenyl Dicofol (1,1-Bis(chlorophenyl)-2,2,2-trichloroethanol) 115-32-2 10501 180.198 Acaricide phosphonate Trichlorfon 52-68-6 57901 180.259 Acaricide sulfite ester Propargite 2312-35-8 97601 180.446 Acaricide tetrazine Clofentezine 74115-24-5 125501 180.448 Acaricide thiazolidine Hexythiazox 78587-05-0 128849 180.517 Acaricide phenylpyrazole Fipronil 120068-37-3 129121 180.566 Acaricide pyrazole Fenpyroximate 134098-61-6 129131 180.572 Acaricide carbazate Bifenazate 149877-41-8 586 180.593 Acaricide unclassified Etoxazole 153233-91-1 107091 180.599 Acaricide unclassified Acequinocyl 57960-19-7 6329 180.341 Acaricide, fungicide dinitrophenol Dinocap (2, 4-Dinitro-6-octylphenyl crotonate and 2,6-dinitro-4- 39300-45-3 36001 octylphenyl crotonate} 180.111 Acaricide, insecticide organophosphorus Malathion 121-75-5 57701 180.182 Acaricide, insecticide cyclodiene Endosulfan 115-29-7 79401
    [Show full text]
  • Use Patterns and Formulations
    PESTICIDE FACT SHEET Name of Chemical: Indaziflam Reason for Issuance: Conditional Registration Date Issued: July 26, 2010 I. DESCRIPTION OF CHEMICAL Chemical Name: Indaziflam; N-[(1R,2S)-2,3-dihydro-2,6-dimethyl-1H-inden-1-yl]-6-[(1RS)-1­ fluoroethyl]-1,3,5-triazine-2,4-diamine Common Name: Indaziflam EPA PC Code: 080818 Chemical Abstracts Service (CAS) Number: 950782-86-2 Year of Initial Registration: 2010 Pesticide Type: Herbicide Chemical Class: Alkylazine Mode of Action: Indaziflam controls weeds by inhibiting cellulose biosynthesis (CB Inhibitor) Registrant: Bayer Environmental Science and Bayer Advanced II. USE PATTERNS AND FORMULATIONS Application Sites: Indaziflam is a selective herbicide providing pre-emergence and post- emergence (when indaziflam is formulated with 2,4-D, dicamba, mecoprop, and penoxsulam) control of annual grasses and broadleaf weeds. Indaziflam is registered for application to residential and commercial areas (lawns, ornamentals, and hardscapes including patios, walkways, etc.), turf (parks, cemeteries, golf courses, sod farms, sports fields, and commercial lawns), field grown ornamentals and Christmas trees, commercial nursery and landscape plantings, and forestry sites. Types of Formulations: Indaziflam is registered as EPA Reg. 432-RLNR (1501) BCS­ AA10717 Technical Herbicide (containing 95.8% indaziflam) and EPA Reg. 432-RUOI (1498) BCS-AA10717 2% MUP Herbicide (containing 2.0% indaziflam). Indaziflam is proposed for use by commercial applicators (formulated in water soluble bags and added to turf fertilizer). These proposed registrations include EPA Reg. 432-RUOO (1499) BCS-AA10717 20WSP Herbicide (containing 20.0% indaziflam), EPA Reg. 432-RUOL (1495) BCS-AA10717 0.0142% Plus Turf Fertilizer Herbicide (containing 0.0142% indaziflam), EPA Reg.
    [Show full text]
  • U.S. EPA, Pesticide Product Label, QUINCLORAC 75 SWF, 02/06/2006
    u.s. ENVIRONM£~J7AL PkO';EC';ION N:JENCY EPfI, Req. Cate ~f Issuance: Office of t'esticide "roqram.<; Number: Keqistratlon Divlsion (7:'()SC) 1200 Pennsylvania Ave., N.W. WashingtrJII, D.::'. ?046D 42750- 131 FEE - 6 2006 NOTICE OF PESTICIDE: Term of Issuance: ~ Registration Conditional __ Reregistration : under r: fRJ'l., as am'?nd'O'd: Name of ~esticide Product: Quinclorac 75DF SWF Name and Address of RegIstrant ,include ZIP Codej: Albaugh, Inc. P.O. Box 2127 Valdosta, GA 31604-2127 Note: Changes in .LabEoli~fg differing in suostance from that accepted in connection with this registration must be submitted to and accepted by the Registratlon Division prior to use of the label in commerce. In any correspondence on this product always refer to the above EPA registration number. em ::he bas':s of lnformat':on f ~rr,lshed by the reg:s'Crant, the above llamed pesticide ':5 hereby roegisterea/reregJ.3terec under :::--.e federa; =nsec::':c:ide, fungicide and Rodenticide Act. Reg':straL,on is ir. no (.Jay tc be ::onstrued as an endorsement or recommendation of this product by the Agency. =n urder to protect hea~ttJ and tr.e ",nvil"onment, ::he Admir.istrator, on his motion, may at any time suspend or cancel the regi3t:::ation of a pesticide in accoraance with the Act. The acceptance of any name 1.n connection with the registration of a product under this Act is not to be construed as giving the registrant a right to -=xclusive use of the r,ame or to its use if it has been coveroed by others.
    [Show full text]